We are a Genomics-as-a-Service company, applying our end-to-end solutions to hand #genetic reports at the #clinical desk. We make #genomics accessible!
We are very happy to announce that CBR Genomics was elected to the TOP 10 EMERGING NEXT-GENERATION SEQUENCING COMPANIES IN EUROPE ๐ ๐๐
https://t.co/01kHGfgDCc
Fabry Disease is a multisystemic pathology, which means that it can affect several systems of our body ๐งโโ๏ธ
Essentially, Fabry Disease manifests in the cardiovascular โค๏ธ neurological ๐ง renal, and gastrointestinal systems ๐ค
#fabry#fabridisease#april#cbrgenomics
Rare diseases are not that rare after all ๐๏ธ
About 70% of rare diseases have a genetic origin ๐งฌ With pan adequate genetic analysis, these diseases can be screened before the appearance of the firsts symptoms.
This is what we aim for with our DNA.files BABY service โ prevent
Statistical data indicates that Fabry Disease affects 1 in 40,000 to 117,000 male births. However, as with almost all rare diseases, the diagnostic capacity is low and the number of real cases is far from the statistics.
#fabry#fabrydiseade#april#awarenessmonth#dna#trends
Fabry disease is a rare and hereditary disease. It is caused by a mutation on the X chromosome and therefore it has a higher effect on males (XY) because they have only one X.
April is "Fabry Disease Awareness Month" and, as such, we launched a new section on this pathology. Throughout the month we will present Fabry Disease and demystify its condition. Ready to join? ๐
#fabry#fabrydiseade#april#awarenessmonth#dna#trends#life#future
The Human Genome has been fully mapped. The research was recently published by Science.
The final code counts with 3 billion letters, an absolutely huge number. If it took us 1 second to type each letter in the human genome, it would take us about 95 years to complete the task ๐คฏ
With our DNA.files BABY service, it is possible to detect mutations in more than 500 genes, responsible for about 300 pediatric diseases of genetic originย ๐งฌ
All of this, before the appearance of the first symptomsย ๐ถ
#baby#pregnant#pregnancy#cbr#dna#heritage#health
At the @WebSummit, we have a Community Room - "The Code of Life" - dedicated to information sessions on #Genetics and the (Future) Present of Personalised #medicine.
๐Join us today at 3:00 pm and 6:40 pm to participate and interact with our experts.
https://t.co/dNVopwuidO